...col1a2 and smad3), serum CRE and BUN content induced by HFD. These findings suggested that dietary lecithin supplementat...
Osteogenesis imperfecta (OI) is mostly caused by pathogenic variants in COL1A1/COL1A2; while single nucleotide variants ...
...COL1A2 (0.5%), COL2A1 (0.5%), GHRHR (0.5%), PTPN11 (0.5%), and SOX3 (0.5%) genes. One patient (0.5%) had a digenic mutat...
...Col1a2, Col3a1, fibronectin-1, tenascin-C) and phenotypic markers (fibroblast activation protein [FAP], podoplanin [PDPN...
...Col1a2 mRNA ratio determines reduced collagen type I production in OI mice bones as the underlying mechanism of haploins...
...COL1A2, resulting in aberrant collagen deposition and ECM remodeling. The remodeled microenvironment in turn facilitates...
...COL1A2, ROBO1) in 18 cases, adding a 10.46 % diagnostic yield. K-means clustering grouped 17 of these genes into three p...
...COL1A2, COL3A1, S100A4, NOTCH1, THY1 and MT-ND2. In addition, the MSTN, COL4A1, COL4A2, SPEN, S100A4, NOTCH1, NOTCH3, an...
...COL1A2, COL4A1, and COL5A2 via the Maximum Clique Centrality (MCC) algorithm. Gene Ontology (GO) and Kyoto Encyclopedia ...
...COL1A2. Significant differences were observed in the pathway scores for epithelial-to-mesenchymal transition, extracellu...
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